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This article is part of the supplement: International Conference on Prevention & Infection Control (ICPIC 2011)

Open Access Poster presentation

Molecular epidemiology of KPC-producing Klebsiella pneumoniae clinical isolates in hospitals in North-Western Tuscany

A Buzzigoli1*, P Valentini12, M Minacori1, F Guarneri12, R Banducci12, C Tascini3, F Menichetti3, GM Rossolini4, B Casini15 and GP Privitera12

  • * Corresponding author: A Buzzigoli

Author Affiliations

1 Experimental Pathology, M.B.I.E., University of Pisa, Pisa, Italy

2 Hygiene and Epidemiology, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy

3 Infectious Diseases, Azienda Ospedaliera Universitaria Pisana, Pisa, Italy

4 Molecular Biology, University of Siena, Siena, Italy

5 Hygiene and Epidemiology, University of Pisa, Pisa, Italy

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BMC Proceedings 2011, 5(Suppl 6):P296  doi:10.1186/1753-6561-5-S6-P296


The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1753-6561/5/S6/P296


Published:29 June 2011

© 2011 Buzzigoli et al; licensee BioMed Central Ltd.

This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Introduction / objectives

The emergence and spread of carbapenem-resistant Enterobacteriaceae represents a major clinical and public health challenge, especially concerning those organisms that produce Klebsiella pneumoniae carbapenemase (KPC)–type b-lactamase. In this study, we examined the molecular epidemiology of KPC-producing Klebsiella pneumoniae strains, isolated during sporadic or epidemic cases in different hospitals of North-Western Tuscany (NWT).

Methods

Starting from April 2010, an outbreak of clinical infection caused by multiresistant Klebsiella pneumoniae, occurred in the University Hospital of Pisa and in other hospitals from the surrounding area; during this period we isolated 57 Klebsiella pneumoniae strains in our hospital and 23 from other health-care facilities; all strains, isolated mostly from different patients hospitalized over protracted periods of time, showed reduced susceptibility to carbapenems and were assayed for KPC detection.

Results

60 out of 61 tested strains produced KPC type 2; molecular typing results indicated the spread of a prevalent clone during the outbreak in Pisa. The PFGE method allowed to identify 7 variants clonally related (pt A1-A7), sharing the same MLST sequence type (ST 258).

Conclusion

Molecular characterization confirmed the higher discriminatory power of PFGE compared to MLST and it may be useful in local and short-time outbreaks; however MLST, providing unequivocal and comparable data, remains the gold standard for molecular typing.

Disclosure of interest

None declared.